FDA Warning Letter — MANDELAY KFT

Case 603799 — FEI 3010452718

The FDA took a Warning Letter action against MANDELAY KFT on February 3, 2020 (Tokol, Hungary). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
MANDELAY KFT
Date
February 3, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Tokol (Hungary)